Investigation of the expression of the C-terminal cross-linking telopeptide of type I collagen (CTXI) in saliva during early and delayed loading of dental implants.

IF 2.6 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Dania Hamid, Shaheen Ahmed, Abdul Hafeez Shaikh, Sadaf Nisar, Raheel Memon, Samreen Malik
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引用次数: 0

Abstract

Background: Implants are commonly used as a treatment choice for partially dentate or edentulous patients. Currently, no specific biomarker for assessing the bone status around dental implants of healthy patients has been reported for evaluating bone deposition, resorption, or stability. CTXI (C-terminal telopeptide of type I collagen) is a known specific biomarker for bone resorption. However, CTXI levels in the saliva of healthy patients with dental implants have not been investigated.

Objectives: This randomized controlled trial aimed to evaluate salivary CTXI levels in dental implant patients with early and delayed loading and to compare them with the values of the periotest to determine implant stability and loading time.

Methods: This study was conducted in Karachi, Pakistan, and included 40 patients with dental implants placed in the posterior mandible. Patients were randomly divided into two groups based on the timing of implant loading: an early loading group, where implants were functionally loaded within 1 month of placement, and a delayed loading group, where implants were loaded after 3 months. The intervention involved functional loading of the implants according to the assigned group. Implant stability was assessed using a periotest on the day of surgery and at 1 month or 3 months, depending on the group. Additionally, saliva samples were collected from all patients at 1 month and 3 months to evaluate CTXI expression levels using sandwich ELISA.

Results: A comparison by periotest showed that dental implants were stable in the early loading group and that osseointegration was good; thus, loading could be applied within one month of dental implant placement. However, in our study, the CTXI bone turnover marker was not detected in any group and thus cannot be used to indicate bone implant stability or loading time.

Conclusion: This study demonstrates that early loading of dental implants can achieve stability and osseointegration within one month, as confirmed by Periotest measurements. However, salivary CTXI levels were undetectable in both early and delayed loading groups, indicating that this biomarker is unsuitable for assessing bone-implant stability or determining the optimal timing for implant loading in healthy patients. These findings suggest further research to explore alternative biomarkers for non-invasive osseointegration and implant stability monitoring.

Trial registration: Retrospectively registered, ID: NCT06246097, Date of registration: 07/02/2024, ( https://clinicaltrials.gov/ct2/show/NCT06246097 ).

I型胶原c端交联末端肽(CTXI)在口腔种植体早期和延迟加载过程中唾液表达的研究
背景:种植体通常被用作部分牙齿或无牙患者的治疗选择。目前,还没有专门的生物标志物用于评估健康患者种植体周围的骨状态,以评估骨沉积、再吸收或稳定性。CTXI (I型胶原c -末端末端肽)是已知的骨吸收特异性生物标志物。然而,尚未调查健康种植牙患者唾液中的CTXI水平。目的:本随机对照试验旨在评估早期和延迟加载牙种植体患者唾液CTXI水平,并将其与牙周膜值进行比较,以确定种植体的稳定性和加载时间。方法:本研究在巴基斯坦卡拉奇进行,包括40例在后下颌种植牙的患者。根据种植体加载时间将患者随机分为两组:早期加载组,种植体在放置后1个月内进行功能加载;延迟加载组,种植体在3个月后加载。干预包括根据指定组植入物的功能负荷。根据组的不同,在手术当天和1个月或3个月时使用骨膜检查来评估种植体的稳定性。此外,在1个月和3个月时收集所有患者的唾液样本,使用夹心ELISA法评估CTXI表达水平。结果:经骨膜检查比较,早期加载组种植体稳定,骨结合良好;因此,可以在种植牙放置后的一个月内进行加载。然而,在我们的研究中,CTXI骨转换标志物未在任何组中检测到,因此不能用于指示骨种植体稳定性或加载时间。结论:本研究表明,早期加载种植体可以在一个月内达到稳定和骨整合,这一点得到了Periotest测量的证实。然而,在早期和延迟加载组中,唾液CTXI水平均未检测到,这表明该生物标志物不适合评估骨植入物稳定性或确定健康患者植入物的最佳时间。这些发现建议进一步研究探索非侵入性骨整合和种植体稳定性监测的替代生物标志物。试验注册:回顾性注册,ID: NCT06246097,注册日期:07/02/2024,(https://clinicaltrials.gov/ct2/show/NCT06246097)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Oral Health
BMC Oral Health DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.90
自引率
6.90%
发文量
481
审稿时长
6-12 weeks
期刊介绍: BMC Oral Health is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of disorders of the mouth, teeth and gums, as well as related molecular genetics, pathophysiology, and epidemiology.
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